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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626808Generated: October 30, 2026

Triethylamine → HCID 178509437, compound

https://huagongshe.com/reaction/626808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-5-bromo-3-chlorobenzonitrileHCID 26598311—
Reactant4-Azido-5-fluoropyridine-3-carbaldehydeHCID 86697053—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
ProductHCID 178509437HCID 178509437—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4-azido-5-fluoropyridine-3-carbaldehyde (3.75 g, 22.6 mmol) and 2-amino-5-bromo-3-chlorobenzonitrile (5.24 g, 22.6 mmol) in DCM (75 mL) was cooled to 0° C. under an atmosphere of nitrogen. Triethylamine (9.5 mL, 68 mmol) was added, followed by titanium (IV) chloride solution (1 N in DCM, 13.6 mL, 13.6 mmol) dropwise. The reaction mixture was stirred at 0° C. for 2 hours and then allowed to reach room temperature overnight. The resultant mixture was concentrated under reduced pressure and the residue was suspended in toluene and filtered through a pad of Celite®. The filtrate was concentrated under reduced pressure to afford the title compound which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309240B2
Source datasetuspto-grants-2016_04
ORD IDord-07827ac237a346afbfbbe4a6a7fe8cb8
Source noteuspto-grants-2016_04